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公开(公告)号:US20240392319A1
公开(公告)日:2024-11-28
申请号:US18670514
申请日:2024-05-21
Applicant: Molecular Transfer, Inc.
Inventor: Gulilat Gebeyehu , Joel Jessee
IPC: C12N15/87 , C07K5/00 , C07K5/068 , C07K5/072 , C07K5/083 , C07K5/087 , C07K5/09 , C07K5/097 , C07K5/11 , C07K7/04 , C07K7/06 , C07K7/08 , C07K14/00
Abstract: Disclosed herein are transfection complexes comprising at least one cell surface ligand; at least one helper lipid component; and a transfection enhancer. Also disclosed are pharmaceutical compositions comprising the disclosed transfection complexes, and a pharmaceutically acceptable carrier. Further, disclosed are methods of transfecting a cell, the method comprising the steps of: obtaining a transfection complex as disclosed; and contacting a cell with the transfection complex.
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公开(公告)号:US12110345B2
公开(公告)日:2024-10-08
申请号:US18231483
申请日:2023-08-08
Applicant: Stealth BioTherapeutics Inc.
Inventor: Scott M. Duncan
CPC classification number: C07K5/1019 , C30B29/58 , C07B2200/13
Abstract: Disclosed are various crystalline salt forms of Boc-D-Arg-DMT-Lys(Boc)-Phe-NH2.
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公开(公告)号:US12006085B2
公开(公告)日:2024-06-11
申请号:US17832612
申请日:2022-06-04
Applicant: 3-D Matrix, Ltd.
Inventor: Masahiro Nohara , Yuya Hasegawa
IPC: C07K1/34 , B65B3/00 , B65B55/04 , B65B55/12 , B65B63/00 , C07K1/36 , C07K7/08 , A61K38/00 , C07K5/103 , C07K5/11
CPC classification number: B65B55/12 , B65B3/003 , B65B55/04 , B65B63/00 , C07K1/34 , C07K1/36 , C07K7/08 , A61K38/00 , C07K5/101 , C07K5/1019
Abstract: The enclosed disclosure describes, among other things, a method including the steps of a first deaerating step in which a mixture comprising peptides is deaerated by lowering the pressure, filtering the mixture through a sterilizing filter; and a second deaerating step, in which the filtrate is deaerated by vibration and lowering the pressure.
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公开(公告)号:US20230398049A1
公开(公告)日:2023-12-14
申请号:US18035840
申请日:2021-11-17
Applicant: Sederma
Inventor: Philippe Mondon , Olivier Peschard , Richard Leroux
CPC classification number: A61K8/64 , C07K5/101 , C07K5/1019 , C07K5/1021 , A61Q19/08 , A61Q19/00
Abstract: They have the general Formula X-(Xaa)nLE(Xaa)m-Z wherein Xaa is selected from L, K, E and D, either n=2 and m=0, or n=1 and m=1, at the N-terminal end X being selected from H, —CO—R1, —SO2-R1 or a biotinoyl group, at the C-terminal end Z being selected from OH, OR1, NH2, NHR1 or NR1R2, and R1 and R2 being selected from an alkyle, aryle, aralkyle, alkylaryl, alkoxy, saccharide and aryloxy, said group having from 1 to 24 carbon atoms. Preferred peptide sequences are X-LKLE-Z and X-ELED-Z. These tetrapeptides stimulate the synthesis of molecules constituting the ECM, in particular collagen 1 and 4, hyaluronic acid and fibronectin, and can be used for a cosmetic treatment, in particular anti-aging, anti-wrinkle and fine lines, to improve the skin mechanical properties, to increase skin density and volume, hydration, and/or to fight against stretch marks, and skin sagging.
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公开(公告)号:US20230279051A1
公开(公告)日:2023-09-07
申请号:US17963697
申请日:2022-10-11
Applicant: Stealth BioTherapeutics Inc.
Inventor: D. Travis Wilson
CPC classification number: C07K5/1019 , A61K38/07 , C07K5/1016 , A61K45/06
Abstract: The disclosure provides methods of preventing, ameliorating or treating disruption of mitochondrial function and symptoms thereof. The methods provide administering aromatic-cationic peptides in effective amounts to prevent, treat or ameliorate the disruption of mitochondrial oxidative phosphorylation in a cell such as that found in a subject suffering from, or predisposed to a mitochondrial disease or disorder. In some embodiments, the methods comprise administering to a subject suffering from, or at risk for a mitochondrial disease or disorder, an effective amount of an aromatic-cationic peptide to subjects in need thereof.
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公开(公告)号:US20230149501A1
公开(公告)日:2023-05-18
申请号:US17493551
申请日:2021-10-04
Applicant: Cornell Research Foundation, Inc.
Inventor: Hazel H. Szeto
CPC classification number: A61K38/07 , A61K38/08 , A61K38/10 , C07K5/1019
Abstract: The invention provides a method for reducing oxidative damage in a mammal, a removed organ, or a cell in need thereof. The method comprises administering an effective amount of an aromatic cationic peptide. The aromatic cationic peptide has (a) at least one net positive charge; (b) a minimum of three amino acids; (c) a maximum of about twenty amino acids, (d) a relationship between the minimum number of net positive charges (pm) and the total number of amino acid residues (r) wherein 3 pm is the largest number that is less than or equal to r+1; (e) a relationship between the minimum number of aromatic groups (a) and the total number of net positive charges (pt) wherein 3a or 2a is the largest number that is less than or equal to pt+1, except that when a is 1, pt may also be 1; and (f) at least one tyrosine or tryptophan amino acid.
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公开(公告)号:US11484607B2
公开(公告)日:2022-11-01
申请号:US17029226
申请日:2020-09-23
Applicant: On Target Laboratories, LLC
Inventor: Sumith A Kularatne
IPC: A61B5/00 , A61B8/00 , A61B10/00 , A61K49/00 , G01N21/64 , C07K5/087 , C07K5/11 , C07K7/06 , C07K5/062 , C07D209/20 , C07K5/083 , G01N33/574 , C07K7/02 , C07K5/072 , C07K5/078 , C07K5/065 , C07K5/09 , G01N33/58 , A61K49/16
Abstract: The present disclosure relates to prostate specific membrane antigen (PSMA) targeted compounds conjugated to near-infra red (NIR) dyes and methods for their therapeutic and diagnostic use. More specifically, this disclosure provides compounds and methods for diagnosing and treating diseases associated with cells and/or vasculature expressing prostate specific membrane antigen (PSMA), such as prostate cancer and related diseases. The disclosure further describes methods and compositions for making and using the compounds, methods incorporating the compounds, and kits incorporating the compounds.
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公开(公告)号:US20220169677A1
公开(公告)日:2022-06-02
申请号:US17618233
申请日:2020-06-10
Applicant: INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) , CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS) , UNIWERSYTET WARSZAWSKI , FONDATION IMAGINE , ASSISTANCE PUBLIQUE - HÔPITAUX DE PARIS , UNIVERSITE DE PARIS
Inventor: Yves Lepelletier , Françoise Raynaud , Aleksandra MISICKA-KESIK , Anna Katarzyna Puszko , Olivier Hermine
Abstract: A number of anti-angiogenic strategies connected with the VEGF signalling pathway are used in current clinical treatment or trial phase, but they either cause adverse effects or are not specific. Various strategies were aimed at identifying peptides inhibiting the VEGF-A165/NRP-1 interaction. A well-known antiangiogenic peptide is the heptapeptide termed “A7R” having the amino acid sequence ATWLPPR, for which various derivatives have been synthesized, which include peptides having the general sequence Lys(hArg)-AA2-AA3-Arg. However, the ability of the known peptides to inhibit the VEGF-A165/NRP-1 interaction was too low for their use as candidate drugs for inhibiting angiogenesis in subjects in need thereof. The present inventors have now conceived a family of novel peptide-like compounds having a nanomolar affinity for NRP-1, which are thus endowed with a powerful capacity to inhibit the VEGF-A165/NRP-1 interaction. These novel peptide-like compounds may be relevantly used as antiangiogenic compounds, especially in subjects affected with cancer.
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公开(公告)号:US20220169676A1
公开(公告)日:2022-06-02
申请号:US17475290
申请日:2021-09-14
Applicant: Washington University
Inventor: James W. Janetka , Zhenfu Han , Peter Harris , Partha Karmakar
IPC: C07K5/09 , C07K5/11 , C07K5/103 , C07K5/097 , G01N33/58 , A61K47/64 , A61K49/00 , A61K51/04 , A61K51/08 , C07B59/00 , C07D277/64 , C07K5/072 , C07K5/078 , C07K5/107 , C07K5/12
Abstract: The present invention generally relates to compounds that are useful for inhibiting one or more of hepatocyte growth factor activator, matriptase, hepsin, Factor Xa, or thrombin. The present invention also relates to various methods of using the inhibitor compounds including treating a malignancy, a pre-malignant condition, or cancer by administering an effective amount of the inhibitor to a subject in need thereof.
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公开(公告)号:US20220105205A1
公开(公告)日:2022-04-07
申请号:US17112497
申请日:2020-12-04
Applicant: Sumith A. Kularatne , Philip Stewart Low , Sakkarapalayam M. Mahalingam , Pravin Gagare
IPC: A61K49/00 , G01N21/64 , C07K5/087 , C07K5/11 , C07K7/06 , C07K5/062 , C07D209/20 , C07K5/083 , G01N33/574 , C07K7/02 , C07K5/072 , C07K5/078 , C07K5/065 , C07K5/09 , G01N33/58
Abstract: The present disclosure relates to prostate specific membrane antigen (PSMA) targeted compounds conjugated to near-infra red (NIR) dyes and methods for their therapeutic and diagnostic use. More specifically, this disclosure provides compounds and methods for diagnosing and treating diseases associated with cells and/or vasculature expressing prostate specific membrane antigen (PSMA), such as prostate cancer and related diseases. The disclosure further describes methods and compositions for making and using the compounds, methods incorporating the compounds, and kits incorporating the compounds.
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